NDC 71746-010-01 - YUMAKI ORIGINAL MINT TOOTH

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
71746-010
Requested NDC
71746-010-01
Package NDCs from labels
71746-010-01, 71746-010-02
Manufacturer
Jeno And Company
Effective date
2017-12-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
YUMAKI ORIGINAL MINT TOOTH - Jeno And CompanyJeno And Company2017-12-07HUMAN OTC DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71746-010-022020-01-31C16284748780-19d75b9cf-eb97-f424-e053-dadaa90a57cee9e39848-2f71-4f32-8bed-b41fc80c5145

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71746-010-01YUMAKI ORIGINAL MINT TOOTH100 g in 1 TUBEPASTE, DENTIFRICE1001
71746-010-02YUMAKI ORIGINAL MINT TOOTH1 in 1 CARTONPASTE, DENTIFRICE11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71746-010YUMAKI ORIGINAL MINT TOOTH (XYLITOL, GREEN TEA LEAF, ASCORBIC ACID, LEVOMENTHOL, PEPPERMINT, AMINOCAPROIC ACID, WATER) PASTE, DENTIFRICE [JENO AND COMPANY]1Legacy NDC, 2 package rows20171207_e9e39848-2f71-4f32-8bed-b41fc80c5145.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 39 of 39 · 764 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
FIND BICHON CLEANSING MASKGLYCERINPioom Cosmetic Co.,ltd50b7db48-7b55-6df4-e054-00144ff88e882017-05-30WarningsExact identifier
unii: PDC6A3C0OX
Eye WashWATERCVS Pharmacy049cee29-7ec2-4d5b-8308-f522acde43a72017-03-29WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Eagle Brand Medicated Roll On RefreshCAMPHOR, MENTHOLBorden Company (Private) Limited567b6820-fb52-630e-e063-6294a90a8bf82015-07-01WarningsExact identifier
unii: AV092KU4JH

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.